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5-(naphthalen-2-yl)pyrimidin-4-amine is a chemical compound with the molecular formula C14H11N3. It is a derivative of pyrimidin-4-amine, featuring a naphthalen-2-yl group attached to the 5th position of the pyrimidine ring. 5-(naphthalen-2-yl)pyrimidin-4-amine is characterized by its aromatic structure, which includes a naphthalene moiety and a pyrimidine ring. It is an organic molecule that can be found in various chemical libraries and is of interest in the field of organic chemistry, potentially for its reactivity or as a building block in the synthesis of more complex molecules. The compound's specific applications or properties are not detailed in this summary, but it is likely to be studied for its potential use in pharmaceuticals, materials science, or as an intermediate in chemical synthesis.

5000-31-7

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5000-31-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5000-31-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,0 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5000-31:
(6*5)+(5*0)+(4*0)+(3*0)+(2*3)+(1*1)=37
37 % 10 = 7
So 5000-31-7 is a valid CAS Registry Number.

5000-31-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-naphthalen-2-ylpyrimidin-4-amine

1.2 Other means of identification

Product number -
Other names HMS2886I23

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5000-31-7 SDS

5000-31-7Downstream Products

5000-31-7Relevant academic research and scientific papers

Palladium-catalyzed cyanomethylation of aryl halides through domino Suzuki coupling-isoxazole fragmentation

Velcicky, Juraj,Soicke, Arne,Steiner, Roland,Schmalz, Hans-Guenther

, p. 6948 - 6951 (2011/06/19)

A one-pot protocol for the cyanomethylation of aryl halides through a palladium-catalyzed reaction with isoxazole-4-boronic acid pinacol ester was developed. Mechanistically, the reaction proceeds through (1) Suzuki coupling, (2) base-induced fragmentation, and (3) deformylation as shown by characterization of all postulated intermediates. Under optimized conditions (PdCl2dppf, KF, DMSO/H2O, 130 °C) a broad spectrum of aryl bromides could be converted into arylacetonitriles with up to 88% yield.

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